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WO2008133342A1 - Composition de résine de polycarbonate - Google Patents

Composition de résine de polycarbonate Download PDF

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Publication number
WO2008133342A1
WO2008133342A1 PCT/JP2008/058298 JP2008058298W WO2008133342A1 WO 2008133342 A1 WO2008133342 A1 WO 2008133342A1 JP 2008058298 W JP2008058298 W JP 2008058298W WO 2008133342 A1 WO2008133342 A1 WO 2008133342A1
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WIPO (PCT)
Prior art keywords
group
carbon atoms
resin composition
formula
represented
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Ceased
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PCT/JP2008/058298
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English (en)
Japanese (ja)
Inventor
Toshiyuki Miyake
Masami Kinoshita
Mizuho Saito
Katsuhiko Hironaka
Eiichi Kitazono
Akimichi Oda
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Teijin Ltd
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Teijin Ltd
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Priority to KR1020097020460A priority Critical patent/KR101460825B1/ko
Priority to CN2008800133557A priority patent/CN101668813B/zh
Priority to US12/597,135 priority patent/US8008381B2/en
Priority to JP2009511923A priority patent/JP5323688B2/ja
Priority to EP08740966A priority patent/EP2141202B1/fr
Publication of WO2008133342A1 publication Critical patent/WO2008133342A1/fr
Anticipated expiration legal-status Critical
Ceased legal-status Critical Current

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    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J5/00—Manufacture of articles or shaped materials containing macromolecular substances
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00—Use of organic ingredients
    • C08K5/0008—Organic ingredients according to more than one of the "one dot" groups of C08K5/01 - C08K5/59
    • C08K5/005—Stabilisers against oxidation, heat, light, ozone
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G64/00—Macromolecular compounds obtained by reactions forming a carbonic ester link in the main chain of the macromolecule
    • C08G64/02—Aliphatic polycarbonates
    • C08G64/0208—Aliphatic polycarbonates saturated
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G64/00—Macromolecular compounds obtained by reactions forming a carbonic ester link in the main chain of the macromolecule
    • C08G64/02—Aliphatic polycarbonates
    • C08G64/0208—Aliphatic polycarbonates saturated
    • C08G64/0216—Aliphatic polycarbonates saturated containing a chain-terminating or -crosslinking agent
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G64/00—Macromolecular compounds obtained by reactions forming a carbonic ester link in the main chain of the macromolecule
    • C08G64/18—Block or graft polymers
    • C08G64/186—Block or graft polymers containing polysiloxane sequences
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G64/00—Macromolecular compounds obtained by reactions forming a carbonic ester link in the main chain of the macromolecule
    • C08G64/20—General preparatory processes
    • C08G64/30—General preparatory processes using carbonates
    • C08G64/305—General preparatory processes using carbonates and alcohols
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L2201/00—Properties
    • C08L2201/02—Flame or fire retardant/resistant
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L2201/00—Properties
    • C08L2201/08—Stabilised against heat, light or radiation or oxydation
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L2201/00—Properties
    • C08L2201/10—Transparent films; Clear coatings; Transparent materials

Definitions

  • the present invention relates to a resin composition containing a polycarbonate resin. More specifically, the present invention relates to a bright resin composition containing a polycarbonate resin made from a biogenic material and having excellent heat resistance, heat stability, moldability, transparency and hue.
  • Polycarbonate resin is a polymer in which aromatic or aliphatic dioxy compounds are linked by carbonic acid ester.
  • polycarbonate resin obtained from 2,2-bis (4-hydroxyphenyl) propane commonly known as bisphenol A
  • PC-A 2,2-bis (4-hydroxyphenyl) propane
  • Polycarbonate resins are generally manufactured using raw materials obtained from petroleum resources.
  • there is concern about the exhaustion of petroleum resources and there is a demand for the practical use of polycarbonate resins using biogenic substances such as plants. Yes.
  • polycarbonate resin strength S using ether diol obtained from carbohydrates as a raw material has been studied. For example, the following formula (a)
  • the ether diol shown in is easily made from sugars and starch. There are three known stereoisomers of this ether diol. Specifically, the following formula (b)
  • isosorbide 6-dianhydro 1-D-sorbitol
  • Isosorbide, isomannide and isoidid are obtained from D-glucose, D-mannose and L-idose, respectively.
  • isosorbide can be obtained by hydrogenating D-glucose and then dehydrating it using an acid catalyst. So far, among the above-mentioned ether diols, in particular, the ability to incorporate into polypolyone using mainly isosorbide as a monomer has been studied. In particular, isosorbide homopolypone is described in Patent Documents 1 and 2 and Non-Patent Documents 1 and 2, respectively.
  • Patent Document 1 proposes a homopolycarbonate resin having a melting point of 20 ° C. obtained by a melt transesterification method.
  • Non-Patent Document 1 also discloses a homopolyester having a glass transition temperature of 16.6 ° C obtained by a melt transesterification method using zinc acetate as a catalyst.
  • a strong Ponate resin has been proposed.
  • This polycarbonate resin has a thermal decomposition temperature (5% weight loss temperature) of 283 ° C., and its thermal stability is not sufficient.
  • Non-Patent Document 2 proposes a method of producing a homopolycarbonate resin by interfacial polymerization using isosorbide bischloroformate. However, the resulting polystrength polyester resin has a glass transition temperature of 144 ° C and is not sufficiently heat resistant.
  • Patent Document 2 proposes a polycarbonate resin having a glass transition temperature of 170 ° C or higher.
  • Patent Document 1 British Patent Application Publication No. 1079686
  • Patent Document 2 International Publication No. 2007/013463 Pamphlet
  • Non-Patent Document 1 "Jou rna l o f App l i e d Po l i e m e Sci enc e", 2002, Vol. 86, p. 872—880
  • Non-Patent Document 2 “Macro omo 1 e c u 1 e s”, 1996, Vol. 29, p. 8077-8082 Disclosure of the Invention
  • an object of the present invention is to provide a resin composition excellent in heat resistance, thermal stability, moldability, hue and transparency. Another object of the present invention is to provide a molded article comprising a resin composition.
  • the present inventor has developed a polyphenol-based resin derived from a saccharide (component A), a heat stabilizer (S component), a phosphorus heat stabilizer (PS) and a hindered phenol heat stabilizer (HS), It was found that a resin composition excellent in heat resistance, thermal stability, hue, and transparency can be obtained by containing at least one compound selected from the group consisting of:
  • At least one compound selected from the group consisting of a nitrogen-containing basic compound, an alkali metal compound, and an alkaline earth metal compound is used as a polymerization catalyst. And found that a carbohydrate-derived polycarbonate resin (component A) having excellent heat resistance, heat stability and moldability can be obtained. Further, when this polycarbonate resin (component A) contains at least one compound selected from the group consisting of a phosphorus-based heat stabilizer (PS) and a hindered phenol-based heat stabilizer (HS) as a heat stabilizer, The present inventors have found that a resin composition having excellent properties, thermal stability, hue, and transparency can be obtained.
  • PS phosphorus-based heat stabilizer
  • HS hindered phenol-based heat stabilizer
  • a resin composition excellent in releasability can be obtained without adding a separate release agent by substituting the terminal of a carbohydrate-derived polycarbonate resin (component A) with a group having a specific structure.
  • the present invention is based on the fact that 100 parts by weight of a polycarbonate resin (component A) mainly containing a repeating unit represented by the following formula (1) is phosphorous heat stabilizer (PS) and hindered phenol heat stability.
  • this invention is a molded article which consists of this resin composition.
  • the polycarbonate resin (component A) used in the present invention is mainly represented by the following formula (1)
  • the repeating unit represented by these is contained.
  • Content of repeating unit represented by formula (1) Is preferably 90 to 100 mol%, more preferably 95 to 100 mol%, and still more preferably 98 to 100 mol%.
  • Particularly preferred is a homopolypolyester resin consisting only of repeating units of the formula (1).
  • the repeating unit represented by the formula (1) is a unit derived from isosorbide (1, 4; 3, 6-dianhydro-D-sorbi) ⁇ ).
  • the other repeating unit is preferably a unit derived from an aliphatic diol or an aromatic bisphenol.
  • the content of other repeating units is preferably 10 to 0 mol%, more preferably 5 to 0 mol%, still more preferably 2 to 0 mol%.
  • the aliphatic diol an aliphatic diol having 2 to 20 carbon atoms is preferable, and an aliphatic diol having 3 to 15 carbon atoms is more preferable. Specific examples include 1,3-propanediol and 1,4-butanediol.
  • Aromatic bisphenols include 2,2-bis (4-hydroxyphenyl) propane (commonly known as “bisphenol A”), 1,1 bis (4-hydroxyphenyl) cyclohexane, 1,1 Bis (4-hydroxyphenyl) 1,3,5,5-trimethylcyclohexane, 2,2-bis (4-hydroxy-3-methylphenyl) propane, 2,2-bis (4-hydroxyphenyl) 1,4-methylpentane, 1,1 And bis (4-hydroxyphenyl) decane.
  • Polycarbonate resin (component A) has a lower limit of the specific viscosity at 20 ° C of a solution of 0.7 g of resin dissolved in 100 ml of methylene chloride, preferably 0.20, more preferably 0.22.
  • the upper limit is preferably 0.45 force S, more preferably 0.37, and still more preferably 0.34.
  • the specific viscosity is lower than 0.20, it becomes difficult to give the molded product obtained from the resin composition of the present invention sufficient mechanical strength.
  • the specific viscosity is higher than 0.445, the melt fluidity becomes too high and the melting temperature having the fluidity necessary for molding becomes higher than the decomposition temperature, which is not preferable.
  • the specific viscosity is preferably 0.20 to 0.45.
  • Polycarbonate resin (component A) has a melt viscosity measured at 250 ° C at 250 ° C with a share rate of 60 0 se C— 1 0.4X 1 0 3 ⁇ 2. Is preferably in the range of 4X 10 3 P a ⁇ s, more preferably within a range of 0. 4X 10 3 ⁇ 1. 8X 1 0 3 Pa ⁇ s. When the melt viscosity is within this range, the mechanical strength is excellent, and when molding using the resin composition of the present invention, there is no generation of silver during molding, which is good.
  • the lower limit of the glass transition temperature (Tg) of the polystrength Ponate resin (component A) is preferably 150 ° C, more preferably 155 ° C, and the upper limit is preferably 200 ° C, more preferably 190 ° C. ° C, more preferably 168 ° C, and particularly preferably 165 ° C or less.
  • the glass transition temperature (Tg) is preferably 150 to 200 ° C. When Tg is less than 150 ° C, the heat resistance (particularly heat resistance due to moisture absorption) is poor, and when it exceeds 200 ° C, the melt fluidity during molding using the resin composition of the present invention is poor. Tg is measured by DSC (model DSC291 0) manufactured by TA Instrunumes.
  • the lower limit of the 5% weight loss temperature (Td) of the polycarbonate resin (component A) is preferably 330 ° C, more preferably 340 ° C, more preferably 350 ° C, and the upper limit is preferably 400 ° C. More preferably, it is 390 ° C, and more preferably 380 ° C.
  • the 5% weight loss temperature (Td) is preferably 330 to 400 ° C. It is preferable that the 5% weight loss temperature is within the above range since there is almost no decomposition of the resin when molding using the resin composition of the present invention.
  • the 5% weight loss temperature (Td) is measured with a TGA (model TGA2950) manufactured by TA I n s t r ume nts.
  • the content of biogenic substances measured according to ASTM D6866 05 of polycarbonate resin (component A) is 50 to 100%, preferably 70 to 100%, more preferably 83 to 100%, and still more preferably. Is 84-100%. (Terminal group)
  • the polystrength Ponate resin (component A) used in the present invention is represented by the following formula (2) or The ability to contain end groups represented by (3)
  • R 1 is an alkyl group having 4 to 30 carbon atoms, an aralkyl group having 7 to 30 carbon atoms, a perfluoroalkyl group having 4 to 30 carbon atoms, or Following formula (4)
  • the number of carbon atoms of the alkyl group for R 1 is preferably 4-22, more preferably 8-22.
  • the alkyl group include a hexyl group, an octyl group, a nonyl group, a decyl group, an undecyl group, a dodecyl group, a pendedecyl group, a hexadecyl group, and a octadecyl group.
  • the number of carbon atoms of the aralkyl group of R 1 is preferably 8-20, more preferably 10-20.
  • Examples of the aralkyl group include benzyl group, phenethyl group, methylbenzyl group, 2-phenylpropane-2-yl group, and diphenylmethyl group.
  • the number of carbon atoms of the perfluoroalkyl group of R 1 is preferably 4-20.
  • 4,4,5,5,6,6,7,7,7-nonafluoro-heptyl group, 4, 4, 5, 5, 6, 6, 7, 7, 8, 8, 9 , 9, 9—Tride decafluoronyl group, 4, 4, 5, 5, 6, 6, 7, 7, 8, 8, 9, 9, 10, 10, 11, 11, 11 Ndecyl group can be mentioned.
  • R 2 , R 3 , R 4 , R 5 and R 6 are each independently an alkyl group having 1 to 10 carbon atoms, a cycloalkyl group having 6 to 20 carbon atoms, or the number of carbon atoms.
  • alkyl group having 1 to 10 carbon atoms in the formula (4) include a methyl group, an ethyl group, a propyl group, a butyl group, and a heptyl group.
  • Examples of the cycloalkyl group having 6 to 20 carbon atoms include a cyclohexyl group, a cyclooctyl group, a cyclohexyl group, and a cyclodecyl group.
  • Examples of the alkenyl group having 2 to 10 carbon atoms include ethenyl group, propenyl group, butenyl group, heptenyl group and the like.
  • Examples of aryl groups having 6 to 10 carbon atoms include phenyl, tolyl, dimethylphenyl, and naphthyl groups.
  • Examples of the aralkyl group having 7 to 20 carbon atoms include benzyl group, phenethyl group, methylbenzyl group, 2-phenylpropane-1-yl group, and diphenylmethyl group.
  • R 2 , R 3 , R 4 , R 5 and R 6 are each independently a group consisting of an alkyl group having 1 to 10 carbon atoms and an aryl group having 6 to 10 carbon atoms. It is preferably at least one group selected from In particular, it is preferably at least one group independently selected from the group consisting of a methyl group and a phenyl group.
  • b is an integer of 0 to 3, preferably an integer of 1 to 3, more preferably an integer of 2 to 3.
  • c is an integer of 4 to 100, more preferably an integer of 4 to 50, and still more preferably an integer of 8 to 50.
  • X in the formula (3) represents at least one bond selected from the group consisting of a single bond, an ether bond, a thioether bond, an ester bond, an amino bond, and an amide bond.
  • X is preferably at least one bond selected from the group consisting of a single bond, an ether bond and an ester bond. Of these, single bonds and ester bonds are preferred.
  • a is an integer of 1 to 5, more preferably an integer of 1 to 3, and still more preferably 1.
  • the terminal group represented by the above formula (2) or (3) is preferably derived from a biogenic substance.
  • biogenic substances include long-chain alkyl alcohols having 14 or more carbon atoms, such as sebutanol, stearyl alcohol, and behenyl alcohol.
  • the content of the end group represented by the formula (2) or (3) is 0.3 to 9% by weight, preferably 0.3 to 7.5% by weight, more preferably 0.5%, based on the polymer main chain. 5 to 6% by weight.
  • the resin composition containing the polystrength monoponate resin (component A) having the above-mentioned end groups is excellent in releasability, and the necessity for adding a release agent is low. For this reason, there is no fear of coloring due to scratches during molding with a release agent.
  • Poly-strength Ponate resin (component A) has a biogenic substance content measured according to AS TM D6866 05 of 50% to 100%, preferably 83% to 100%, resin 0.7 g
  • the specific viscosity at 20 ° C of a solution in which 100 ml of methylene chloride is dissolved is 0.20 to 0.45
  • the glass transition temperature (T g) is 150 to 200 ° C
  • the 5% weight loss temperature (Td) is preferably 330 to 400 ° C.
  • Polycarbonate resin (component A) is represented by the following formula (a)
  • isosorbide isomannide, and isoidid.
  • saccharide-derived ether diols are also obtained from natural biomass and are one of the so-called renewable resources.
  • Isosorbide is obtained by hydrogenating D-glucose obtained from starch and then dehydrating it.
  • Other ether diols can be obtained by the same reaction except for the starting materials.
  • isosorbide (1,4; 3,6-dianhydro-D-sorbyl) represented by the formula (b) is particularly preferable.
  • Isosorbide is an ether diol that can be easily made from starch, etc., and can be obtained in abundant resources.
  • isomannide is easy to manufacture, has properties, and has a wider range of applications than isoidid. Is excellent.
  • copolymerized with other aliphatic diols or aromatic bisphenols may be copolymerized with other aliphatic diols or aromatic bisphenols as long as the properties of the polycarbonate resin are not impaired.
  • the copolymerization ratio of such other aliphatic dials or aromatic bisphenols is preferably 5 to 0 mol%, more preferably 2 to 0 mol%.
  • an aliphatic diol having 2 to 20 carbon atoms is preferable, and an aliphatic diol having 3 to 15 carbon atoms is more preferable.
  • linear diols such as 1,3-propanediol, 1,4 monobutanediol, 1, ⁇ monopentanediol, 1,6 monohexane diol, cyclohexanediol, cyclohexane
  • alicyclic alkylenes such as xanthanimethanol and the like are mentioned, and among them, 1,3-propandiol, 1,4-monobutanediol, 1,6-hexanediol, and cyclohexanediol are preferred.
  • Aromatic bisphenols include 2,2-bis (4-hydroxyphenyl) puff bread (commonly called “bisphenol ⁇ ”), 1, 1 bis (4-hydroxyphenyl) Cyclohexane, 1, 1 bis (4-hydroxyphenyl) 1, 3, 3, 5-trimethylcyclohexane, 4, 4 '— (m-phenylene diisopropylidene) diphenol, 9, 9 bis (4-hydroxy-1-methylphenyl) fluorene, 2,2-bis (4-hydroxy-3-methylphenyl) propane, 2,2-bis (4-hydroxy-1-methylphenyl) propane, 2,2-bis (4-hydroxyphenyl) ) 4-methylpentane, 1,1-bis (4-hydroxyphenyl) decane, 1,3-bis ⁇ 2- (4-hydroxyphenyl) propyl ⁇ benzen and the like.
  • other diol residues may be included, and examples thereof include aromatic diols such as dimethanol benzene and diethanol benzene.
  • the polycarbonate resin (component A) containing a terminal group represented by the formula (2) or (3) is used with respect to the ether diol, carbonic acid diester and ether diol represented by the formula (a).
  • a melt compound that is mixed with a hydroxy compound represented by the following formula (e) or (f) and distills alcohol or phenol produced by transesterification under high temperature and reduced pressure. Can be obtained by performing.
  • Examples of the carbonic acid diester include esters such as aryl groups or aralkyl groups having 6 to 12 carbon atoms which may be substituted with hydrogen atoms, or alkyl groups having 1 to 4 carbon atoms.
  • Specific examples include diphenyl carbonate, bis (diphenyl) carbonate, m-cresyl carbonate, dinaphthyl carbonate, bis (diphenyl) carbonate, dimethyl carbonate, jetyl carbonate, and dibutyl carbonate. But in terms of reactivity and cost Lucaponate is preferred.
  • the amount of the carbonic acid diester is preferably 1.02 to 0.98 mol, more preferably 1.01 to 0.98 mol, and even more preferably 1.0 1 to 0 mol per mol of the ether diol. 9 9 moles. If the molar ratio of the carbonic acid diester is more than 1.02, it is not preferable because the carbonic acid ester residue acts as a terminal block and a sufficient degree of polymerization cannot be obtained. Even when the molar ratio of carbonic acid diester is less than 0.98, a sufficient degree of polymerization cannot be obtained, which is not preferable.
  • Melt polymerization can be carried out by mixing ether diol and carbonic acid diester in the presence of a polymerization catalyst and distilling alcohol or phenol produced by transesterification under high temperature and reduced pressure.
  • the reaction temperature is preferably as low as possible in order to suppress the decomposition of the ether diol and obtain a highly viscous resin with little coloration.
  • the polymerization temperature is 1 8 0 to allow the polymerization reaction to proceed appropriately.
  • the force S is preferably in the range of ° C to 280 ° C, more preferably in the range of 180 ° C to 260 ° C.
  • the polymerization catalyst it is preferable to use at least one selected from the group consisting of a nitrogen-containing basic compound, an alkali metal compound, and an alkaline earth metal compound.
  • the alkali metal compound include sodium hydroxide, potassium hydroxide, sodium carbonate, potassium carbonate, sodium hydrogencarbonate, sodium salt or potassium salt of divalent phenol.
  • alkaline earth metal compounds include 7K calcium oxide, barium hydroxide, and magnesium hydroxide.
  • Nitrogen-containing basic compounds include tetramethylammonium hydroxide, tetraethylammonium hydroxide, tetraptylammonium hydroxide, trimethylamine, and trimethylamine. Ethylamine and the like can be mentioned. These may be used alone or in combination of two or more. Among these, it is preferable to use a nitrogen-containing basic compound and an alkali metal compound in combination.
  • the amount of the polymerization catalyst, to the carbonic acid diester to 1 mole respectively preferably rather the 1 X 1 0 one 9 ⁇ 1 X 1 0- 3 equivalents, more preferably 1 X 1 0- 8 ⁇ 5 X 1 0 — Selected within a range of 4 equivalents.
  • the reaction system is preferably maintained in an atmosphere of a gas that is inert with respect to raw materials such as nitrogen, reaction mixtures, and reaction products. Examples of inert gases other than nitrogen include argon. Furthermore, additives such as antioxidants may be added as necessary.
  • the polystrength Ponate resin (component A) uses at least one compound selected from the group consisting of nitrogen-containing basic compounds, alkali metal compounds, and alkaline earth metal compounds as a polymerization catalyst. a) The ether diol represented by a) and the carbonate diester-forming compound are heated and reacted at normal pressure, and then subjected to melt polycondensation while heating at a temperature of 180 ° C. to 28 ° C. under reduced pressure. it force s preferably one obtained.
  • the C 1 content of the polycarbonate resin (component A) is preferably 0 to 50 ppm, more preferably 0 to 30 ppm, and still more preferably 0 to 10 ppm.
  • the C 1 content of the polycarbonate resin is measured by oxidative decomposition and coulometric titration using a quartz tube combustion method using an all-organic halogen analyzer (T ⁇ X—100 type manufactured by Diain Sturment Co., Ltd.). be able to.
  • the water content of the polycarbonate resin is preferably 0 to 500 ppm, more preferably 0 to 300 ppm.
  • the amount of water in the polycarbonate resin can be measured by a force Luffier one titration method using a moisture vaporizer and a trace moisture measuring device (Miryo Chemical Co., Ltd.).
  • the C 1 content of the polystrength Ponate resin (component A) is 0 to 50 ppm and the water content is 0 to 500 ppm.
  • a resin composition of the present invention is produced by a melt extrusion method or the like using a polycarbonate resin (component A) having a C 1 content and a water content in such a range, a resin composition having a good hue Can be obtained.
  • a polystrength monoponate resin by a melt polymerization method.
  • it is dissolved in a halogen-based solvent and purified by reprecipitation with methanol.
  • a polycarbonate resin it is not preferable to produce a polycarbonate resin by a solution method in which polymerization is carried out in a halogen solvent using an acid binder such as pyridine.
  • an acid binder such as pyridine.
  • the resin composition of the present invention comprises at least one heat stabilizer (S component) selected from the group consisting of a phosphorus heat stabilizer (PS) and a hindered phenol heat stabilizer (HS). 0.5 parts by weight, preferably 0.001 to 0.3 parts by weight, more preferably 0.01 to 0.3 parts by weight.
  • S component selected from the group consisting of a phosphorus heat stabilizer (PS) and a hindered phenol heat stabilizer (HS).
  • the resin composition of the present invention preferably contains a phosphorous heat stabilizer (PS).
  • PSD phosphorous heat stabilizer
  • the phosphorus-based heat stabilizer (PS) is preferably a compound having a structure represented by the following formula (5).
  • R 7 is a hydrogen atom or an alkyl group having 1 to 10 carbon atoms, more preferably a hydrogen atom or an alkyl group having 1 to 4 carbon atoms, particularly a hydrogen atom, a methyl group, An isopropyl group, an isobutyl group, a tert-butyl group, or a tert-pentyl group is preferred.
  • R 8 is an alkyl group having 4 to 10 carbon atoms, preferably an alkyl group having 4 to 6 carbon atoms, particularly preferably an isobutyl group, a tert-butyl group, a tert-pentyl group, or a cyclohexyl group.
  • R 9 is a hydrogen atom, an alkyl group having 1 to 10 carbon atoms, an alkyl group having 1 to 10 carbon atoms.
  • the phosphorus-based heat stabilizer is composed of compounds represented by the following formulas (6), (7) and (8): At least one compound selected from the group is preferred.
  • Preferred examples of the above formula (6) include ⁇ ris (2-isobutylphenyl) phosphate, tris (2-tert-butylphenyl) phosphite, tris (2-tert-pentylphenyl) phosphite, ⁇ ris ( 2-cyclohexylphenyl) phosphite, tris (2, 4-di-tert-butylphenyl) phosphite, tris (2, 6-di-tert-butylphenyl) phosphite, tris (2-tert-butyl-6- Methylphenyl) phosphite.
  • Tris (2,4-ji tert-butylphenyl) phosphite is preferred.
  • Preferred examples of the above formula (7) include tetrakis (2, 4-di-tert- (Ptylphenyl) -4,4'-biphenyl dirange phosphonite, tetrakis (2,4-ji tert-butylphenyl) 1,4,3, bibidiylene phosphonite, tetrakis (2,4-di-tert-butylphenyl) one 3, 3'-biphenylenediphosphonite, tetrakis (2, 6-di-tert-butylphenyl) 1-4, 4-biphenylendiphosphonite, tetrakis (2, 6-ditert-butylphenyl) 1, 4, 3, bibidirange Phosphonite, tetrakis (2, 6-g tert-butylphenyl) 1,3'-biphenyl dirange phosphonite.
  • tetrakis (2,4-di-tert-butylphenyl)
  • X 2 is an alkyl group having 5 to 18 carbon atoms, preferably an alkyl group having 8 to 18 carbon atoms, and particularly preferably an alkyl group having 10 to 18 carbon atoms.
  • dihexyl pen evening erythritol diphosphite Dioctylpentaerythritol I ⁇ Ludiphosphite, dicyclohexylpenite erythritol 1 Rudiphosphite, didecylpentaerythritol 1 Rudiphosphite, didodecylpentaerythritol diphosphite, distearyl pentaerythritol monoludiphosphite, especially distearyl Pentaerythritol diphosphite is preferred.
  • the compound of S component may be one kind or a mixture of two or more kinds.
  • the content of the phosphorus stabilizer (PS) is preferably 0.001 to 0.5 parts by weight, more preferably 0.005 to 0.5 parts by weight per 100 parts by weight of the polycarbonate resin (component A). Parts, more preferably 0.005 to 0.3 parts by weight, particularly preferably 0.01 to 0.3 parts by weight.
  • the phosphorus stabilizer (PS) is within this range, it is possible to suppress a decrease in molecular weight or a deterioration in hue when the resin composition of the present invention is molded.
  • the resin composition of the present invention preferably contains a hindered phenol heat stabilizer (HS).
  • the hindered phenol thermal stabilizer (HS) is preferably a compound containing a structure represented by the following formula (10) (hereinafter referred to as “one X 3 ” group).
  • R 11 is a hydrogen atom or an alkyl group having 1 to 10 carbon atoms, more preferably a hydrogen atom or an alkyl group having 1 to 4 carbon atoms, particularly a methyl group, an ethyl group, or an isopropyl group.
  • An isobutyl group and a tertbutyl group are preferable.
  • R 12 is an alkyl group having 4 to 10 carbon atoms, preferably an alkyl group having 4 to 6 carbon atoms, and particularly preferably an isobutyl group, a tertbutyl group, or a cyclohexyl group.
  • R 13 is a hydrogen atom, an alkyl group having 1 to 10 carbon atoms, an alkoxy group having 1 to 10 carbon atoms, a cycloalkyl group having 6 to 20 carbon atoms, a cycloalkoxy group having 6 to 20 carbon atoms, a carbon atom A group consisting of an alkenyl group having 2 to 10 carbon atoms, an aryl group having 6 to 10 carbon atoms, an aryloxy group having 6 to 10 carbon atoms, an aralkyl group having 7 to 20 carbon atoms and an aralkyloxy group having 7 to 20 carbon atoms Is at least one group selected from Hydrogen atom, alkyl group having 1 to 10 carbon atoms, cycloalkyl group having 6 to 20 carbon atoms, alkenyl group having 2 to 10 carbon atoms, aryl group having 6 to 10 carbon atoms, and 7 to 20 carbon atoms Of these, at least one group selected from the group consisting of aralky
  • the hindered phenol thermal stabilizer (HS) is composed of the compounds represented by the following formulas (11), (12) and (13). At least one compound selected from the group is preferred.
  • R 14 is a hydrocarbon group that may contain an oxygen atom having 8 to 30 carbon atoms, more preferably a hydrocarbon group that may contain an oxygen atom having 12 to 25 carbon atoms.
  • a hydrocarbon group which may contain an oxygen atom having 15 to 25 carbon atoms is preferred.
  • Preferred examples of the above formula (11) include octyldecyl-3- (3,5-diter 1: -butyl-4-hydroxyphenyl) propaneone, benzenepropanoic acid 3,5-bis (1, 1 -Dimethylethyl) 4-hydroxyalkyl ester (alkyl has 7 to 9 carbon atoms and side chain), ethylene bis (oxchethylene) bis [3- (5-tert-butyl-4-hydroxy-m-tolyl) propionate], Hexamethylenebis [3- (3,5-di-tert-butyl-4-hydroxyphenyl) propionate.
  • R 15 is a hydrogen atom or an alkyl group having 1 to 25 carbon atoms, more preferably a hydrogen atom or an alkyl group having 1 to 18 carbon atoms, particularly an alkyl having 1 to 18 carbon atoms. Groups are preferred.
  • m is an integer of 1 to 4, an integer of 1 to 3 is preferable, and 2 is particularly preferable.
  • k is an integer of 1 to 4, 3 to 4 is preferable, and 4 is particularly preferable.
  • Preferable specific examples of the formula (12) include pen erythritol tetrakis [3- (3,5-g-tert-petitul 4-hydroxyphenyl) propionate].
  • “one X 3 ” is a group represented by the formula (10).
  • R 16, R 1 7, R 18 and R 19 are each independently a hydrogen atom or aralkyl Kill group having a carbon number of 1-4, preferably an alkyl group having 1 to 4 carbon atoms, especially methyl force S I like it.
  • p is an integer of 1 to 4, an integer of 1 to 3 is preferable, and 2 is particularly preferable.
  • Preferred examples of formula (13) include 3, 9-bis [2- [3- (3- tert-butyl_4-hydroxy-5_methylphenyl) propiodioxy] 1,1,1-dimethylethyl] —2, 4 , 8, 10-Tetraoxaspiro [5, 5] undecane.
  • Penyu Erythritol Tetrakis [3- (3,5-Di-tert-Petilu 4-Hydroxyphenyl) propionate], Octadecyl 3— (3,5-di-tert-butyl-4-hydroxyphenyl) propionate, 3, 9-bis [2- [3- (3- (tert-butyl-4-hydroxy-5-methylphenyl) propionyloxy 1,1-dimethylethyl] 1,2,4,8,10-tetraoxaspiro [5,5] undecane is particularly preferred.
  • Such a hindered phenol heat stabilizer may be one or a mixture of two or more.
  • hindered phenol thermal stabilizer is preferably a compound represented by the following formula (14).
  • R 21 is an alkyl group having 4 to 10 carbon atoms
  • R 22 is an alkyl group having 1 to 10 carbon atoms
  • R 23 and R 24 are independently hydrogen atoms. Selected from the group consisting of an alkyl group having 1 to 10 carbon atoms; an alkyl group having 2 to 10 carbon atoms, an alkenyl group having 2 to 10 carbon atoms, an aryl group having 6 to 10 carbon atoms, and an aralkyl group having 7 to 20 carbon atoms.
  • R 25 is a hydrogen atom, an alkyl group having 1 to 10 carbon atoms, an alkenyl group having 2 to 10 carbon atoms, an aryl group having 6 to 10 carbon atoms, or 7 to 20 carbon atoms. And at least one group selected from the group consisting of an optionally substituted acryloyl group and an optionally substituted methacryloyl group.
  • R 21 is an alkyl group having 4 to 10 carbon atoms, preferably an alkyl group having 4 to 6 carbon atoms, particularly an isobutyl group, a tert-butyl group, a tert-pentyl group, or a cyclohexyl group.
  • Xylyl basic strength S is preferred.
  • R 22 is an alkyl group having 1 to 10 carbon atoms, preferably an alkyl group having 1 to 4 carbon atoms, particularly a methyl group, an ethyl group, an isopropyl group, an isobutyl group, or a tert-butyl group. Is preferred.
  • R 23 and R 24 are each independently a hydrogen atom, an alkyl group having 1 to 10 carbon atoms, an alkenyl group having 2 to 10 carbon atoms, or 6 to carbon atoms: an aryl group of L 0 and a carbon atom number of 7 Is at least one group selected from the group consisting of -20 aralkyl groups, preferably a hydrogen atom, an alkyl group having 1 to 10 carbon atoms, or an aryl group having 6 to 10 carbon atoms, particularly a hydrogen atom, or Alkyl groups having 1 to 10 carbon atoms are preferred.
  • R 25 is a hydrogen atom, an alkyl group having 1 to 10 carbon atoms, an alkenyl group having 2 to 10 carbon atoms, an aryl group having 6 to 10 carbon atoms, an aralkyl group having 7 to 20 carbon atoms, It is at least one group selected from the group consisting of an optionally substituted acryloyl group and an optionally substituted methacryloyl group, a hydrogen atom, an alkyl group having 1 to 10 carbon atoms, and a carbon number of 7 to Twenty aralkyl groups, an optionally substituted acryloyl group, or an optionally substituted methacryloyl group are preferable, and a hydrogen atom, an acryloyl group, or a methacryloyl group is particularly preferable.
  • hindered phenol thermal stabilizer represented by the formula (14)
  • examples of the hindered phenol thermal stabilizer include 2,2, -methylenebis (6-tert-butyl-4-methylphenol, 2,2′-isopropylidenebis (6- tert-butyl-4-methylphenol, 2-tert-butyl-6- (3-tert-butyl-2-hydroxy-5-methylbenzyl) 4-methyl acrylate, 2-tert-pentyl 6- (3-tert-pentyl- 2-Hydroxy-5-methylbenzyl) 1-4-methylphenyl acrylate, 2-tert-butyl-6- (3-tert-butyl-2-hydroxy-5-methylbenzyl) 1-4-methylphenyl methacrylate, 2-tert-pentyl 6— (3— tert-pentyl mono 2-hydroxy mono 5-methylbenzyl) mono 4-methylphenyl chloride, 2-— [1— (2-hydroxy-3, 5— -Tert-butylphenyl)
  • Such compounds may be one kind or a mixture of two or more kinds.
  • the content of the hindered phenol-based heat stabilizer (HS) is preferably 0.0005 to 0.1 parts by weight, more preferably 0.001 to 0.000 parts per 100 parts by weight of the polycarbonate resin (component A).
  • HS hindered phenol-based heat stabilizer
  • the resin composition of the present invention may contain a release agent (L component).
  • the mold release agent (L component) used in the present invention is an ester of alcohol and fatty acid.
  • the alcohol include monohydric alcohols and polyhydric alcohols.
  • the number of carbon atoms of the alcohol is preferably 1-25, more preferably 1-20, and even more preferably 1-10.
  • the number of carbon atoms of the fatty acid is preferably 10-30, more preferably 10-20.
  • the fatty acid is preferably a saturated fatty acid.
  • Examples of the L component include esters of monohydric alcohols and fatty acids.
  • An ester of a monohydric alcohol having 1 to 20 carbon atoms and a saturated fatty acid having 10 to 30 carbon atoms is preferred.
  • Specific examples include stearyl stearate, palmityl palmitate, butyl stearate, methyl laurate, and isopropyl palmitate.
  • the esterification rate of the release agent (component L) is preferably 10 to 100%, more preferably 25 to 100%, still more preferably 25 to 75%, and particularly preferably 25 to 5%. 0% is used. Use of a release agent having an esterification rate within the above range is preferable in terms of moldability (release property) and transparency.
  • the esterification rate was determined by measuring 1 H-NMR in deuterated chloroform solution using J NM-AL 4 00 made by JEOL, and forming an ester bond in the release agent. Proton (3.6 to 4.0) on carbon bound to an alcohol group not forming an ester bond with a proton on carbon bound to the group (around 4.2 to 5.2 ppm) The ratio of esterification can be obtained from the integral ratio with (ppm).
  • L component examples include partial esters of polyhydric alcohols and fatty acids.
  • the partial ester means that a part of the hydroxyl group of the polyhydric alcohol remains without undergoing ester reaction with the fatty acid.
  • a partial ester of a polyhydric alcohol having 1 to 25 carbon atoms and a saturated fatty acid having 10 to 30 carbon atoms is preferred.
  • Examples of the L component include all ester strengths of polyhydric alcohols and fatty acids.
  • the total ester means that all the hydroxyl groups of the polyhydric alcohol are ester-reacted with the fatty acid.
  • Preference is given to all esters of polyhydric alcohols having 1 to 25 carbon atoms and saturated fatty acids having 10 to 30 carbon atoms.
  • the L component is preferably a partial ester of a polyhydric alcohol and a fatty acid, a full ester, or a mixture thereof.
  • the L component is more preferably a monoester of a polyhydric alcohol and a fatty acid. Partial ester of polyhydric alcohol and fatty acid This has the advantage that the transparency of the molded product is higher than that of the mold.
  • partial esters or total esters of polyhydric alcohols and saturated fatty acids include glycerin monostearate, glycerin distearate, glycerin tristearate, glycerin monobehenate, pen erythritol monostearate, pen Evening erythritol distearate, pen evening erythritol 1, monotetrastearate, pentaerythritol tetrapelargonate, propylene glycol monostearate, biphenyl biphenate, sorbitan monostearate, 2-ethyl hexyl stearate, dipentaerythritol) Dipentyl ester such as stearate!
  • glycerol monostearate glycerol distearate, glycerol monobehenate, pentaerythritol] ⁇ one monostearate, pen erythritol 1 ⁇ one distearate, propylene glycol monostearate, Partial esters such as Sorbi evening monostea lei are preferred. More preferred are glycerin monostearate, pen erythritol mono-monostearate, and pen erythritol mono-stearate. In particular, glycerin monostearate is preferred.
  • the L component compound may be one kind or a mixture of two or more kinds.
  • the content of the release agent (component L) is from 0.1 to 0.5 parts by weight, preferably from 0.03 to 0.5 parts by weight, based on 100 parts by weight of the polycarbonate resin (component A). More preferably, it is 0.03 to 0.3 part by weight, and particularly preferably 0.03 to 0.2 part by weight. When the release agent is within this range, it is possible to improve the release property while suppressing the opaqueness.
  • the production method is not particularly limited.
  • a preferred method for producing the resin composition of the present invention is a method of melt-kneading each component using an extruder.
  • a twin-screw extruder is particularly suitable, and an extruder having a vent capable of degassing moisture in the raw material and volatile gas generated from the melt-kneaded resin can be preferably used.
  • a vacuum pump is used to efficiently discharge the generated moisture and volatile gas from the vent to the outside of the extruder. Is preferably installed.
  • the supply method of the S component and other additives (simply referred to as “additive” in the following examples) to the extruder is not particularly limited, but the following methods are typically exemplified.
  • Another premixing method is a method in which a resin and additives are uniformly dispersed in a solvent and then the solvent is removed.
  • the resin composition extruded from the extruder is directly cut into pellets, or after forming the strands, the strands are cut with a pelletizer to be pelletized. Furthermore, when it is necessary to reduce the influence of external dust, it is preferable to clean the atmosphere around the extruder. Furthermore, in the manufacture of such pellets, the pellet shape distribution is narrowed, miscuts are reduced, and transported using various methods already proposed for optical disc polyphonic resin for optical discs and cyclic polyolefin resin for optical discs. Alternatively, it is possible to appropriately reduce the fine powder generated during transportation and reduce the bubbles (vacuum bubbles) generated in the strands and pellets. These formulations can increase the molding cycle and reduce the rate of defects such as silver.
  • the pellet may have a general shape such as a cylinder, a prism, and a sphere, but is more preferably a cylinder.
  • the diameter of such a cylinder is preferably 1 to 5 mm, more preferably 1.5 to 4 mm, and even more preferably 2 to 3.3 mm.
  • the length of the cylinder is preferably 1 to 30 mm, more preferably 2 to 5 m. m, more preferably 2.5 to 3.5 mm.
  • the resin composition of the present invention can be manufactured into various molded products by injection molding the pellets produced as described above.
  • the resin melt-kneaded by an extruder can be directly made into a sheet, film, profile extrusion molded product, direct blow molded product, and injection molded product without going through the pellets.
  • injection molding not only ordinary molding methods but also injection compression molding, injection press molding, gas assist injection molding, foam molding (including supercritical fluid injection), insert molding, depending on the purpose as appropriate. Molded products can be obtained using injection molding methods such as plastic mold molding, heat insulation mold molding, rapid heating / cooling mold molding, two-color molding, sandwich molding, and ultra-high speed injection molding. The advantages of these various molding methods are already widely known. For molding, either a cold runner method or a hot runner method can be selected.
  • the resin composition of the present invention can also be used in the form of various modified extrusion molded products, sheets, films, and the like by extrusion molding. Inflation, force-rendering, and casting methods can also be used to form sheets and films. Furthermore, it can be formed as a heat-shrinkable tube by applying a specific stretching operation.
  • the resin composition of the present invention can be formed into a molded product by rotational molding or blow molding.
  • a molded article formed from the resin composition of the present invention is excellent in transparency and hue.
  • the haze measured by JISK 7105 of a flat plate having an arithmetic average surface roughness (R a) of 0.03 zm or less and a thickness of 2 mm formed from the resin composition of the present invention is preferably Is 0 to 20%, more preferably 0 to 15%.
  • the b value is preferably in the range of 0 to 14, more preferably in the range of 0 to 13 and even more preferably in the range of 0 to 12.
  • the b value can be measured using a spectrochromator S E—200 (produced by Nippon Denshoku Co., Ltd.) (light source: CZ 2).
  • various function-imparting agents may be added to the resin composition of the present invention, for example, plasticizers, light stabilizers, heavy metal deactivators, flame retardants, lubricants, antistatic agents, UV absorbers and the like.
  • various organic and inorganic fillers, fibers and the like can be used in combination in the resin composition of the present invention depending on the application.
  • the filler include carbon, talc, my strength, wollastonite, montmorillonite, and hyde mouth talcite.
  • the fibers include natural fibers such as kenaf, various synthetic fibers, glass fibers, quartz fibers, and carbon fibers.
  • the resin composition of the present invention includes, for example, polylactic acid, aliphatic polyester, aromatic polyester, aromatic polycarbonate, polyamide, polystyrene, polyolefin, polyacrylic, ABS, polyurethane, and other various biogenic substances. It can also be used by being alloyed with a polymer, a synthetic resin, or rubber.
  • the biogenic substance content rate was measured from the biogenic substance content rate test with the concentration of radioactive carbon (percentm or de rn car bon; C 14).
  • the CI content in the pellets was measured by oxidative decomposition and coulometric titration with a quartz tube combustion method using TOX-100, an all-organic halogen analyzer manufactured by Dia Instruments.
  • the amount of residual water in the pellets was measured by a forceful Fischer one titration method using a moisture vaporizer and a trace moisture measuring device manufactured by Mitsubishi Chemical Corporation.
  • Peretto was dissolved in methylene chloride and the concentration was 15% by weight, and it was placed in a sample tube with a 30 mm path length. Next, it was measured using a color difference meter 30 OA at 20 ° C.
  • the b value is derived from the Hunter's color difference formula based on the tristimulus values X, Y, and ⁇ specified in JISZ 8722. The lower the value, the closer the hue is to colorless.
  • JEOL JNM-AL400 was used to measure 1 H-NMR in pellets in a heavy chloroform solution, and terminal modification was performed based on the integration ratio of specific protons derived from ether diol and terminal hydroxy compounds. The group content was determined. The terminal modification group content was determined from the following formula (1).
  • Terminal modified group content [R t] X X 100 (wt%)
  • Re Composition ratio of ether diol in the main chain determined from iH-NMR integral ratio.
  • Thickness of 3-stage plate (arithmetic mean surface roughness R a; 0.03 m) formed by the method described in the examples. Measurement was performed using 0 (light source: C / 2).
  • the b value is derived from the Hunter's color difference formula from the tristimulus values X, ⁇ , and ⁇ specified in JISZ 8722. The lower the value, the closer the hue is to colorless.
  • Three-stage plate mold (arithmetic mean surface roughness R a;
  • Bending specimens were molded using 75E I I I at a cylinder temperature of 250 ° C and a mold temperature of 90 ° C. The bending test was carried out according to IS 0178.
  • the pressure in the reaction vessel was gradually reduced over 30 minutes, and the pressure was reduced to 13.3 ⁇ 10 3 MPa while distilling off the generated phenol.
  • the temperature was raised to 200 ° C, then the pressure was gradually reduced over 20 minutes, and the methanol was distilled off at 4.00 x 10 to 3 MPa for 20 minutes.
  • the reaction was further performed, and the temperature was raised to 220 ° C. for 30 minutes and then to 250 ° C. for 30 minutes.
  • the resin composition shown in Table 1 was prepared as follows. The ingredients in the proportions shown in Table 1 were weighed and mixed uniformly in the blender. The mixture was dissolved in methylene chloride to a concentration of 15% by weight. The b value of this solution was measured. The evaluation results are shown in Table 1. Examples 12-20
  • the resin composition shown in Table 2 was prepared as follows. Each component in the ratio shown in Table 2 was weighed and mixed uniformly, and the mixture was put into an extruder to prepare a resin composition.
  • a vent type twin screw extruder KZW15-25MG manufactured by Technobel Co., Ltd.
  • the extrusion conditions were a discharge rate of 14 kg / h, a screw rotation speed of 250 rpm, a vacuum pressure of 3 k Pa in the ben bowl, and an extrusion temperature of 250 from the first supply port to the die part to obtain pellets. .
  • the obtained pellets were dried at 100 ° C for 12 hours, and then a mold with a cavity surface with an arithmetic average roughness (Ra) of 0.03 m was used.
  • An injection molding machine [manufactured by Nippon Steel Works, Ltd. J SWJ—75E III], injection molding at cylinder temperature 250 ° C, mold temperature 90 ° C, width 55mm, length 90mm, thickness from the gate side 3mm (length 20mm), 2mm (length A three-stage plate having a thickness of 45 mm) and lmm (length 25 mm) was molded, and the mold release property and the shape of a molded plate having a thickness of 2 mm were visually evaluated. In addition, the hue and Haze of the molded plate were evaluated.
  • the flexural modulus of the molded plate obtained in Example 12 was 3,64 OMPa, the mechanical strength was good, the deflection temperature under load was 151 ° C, and the heat resistance was also excellent. .
  • the raw materials used in Table 1 are as follows.
  • A-1 The polycarbonate resin pellet produced in Reference Example 1 was dried at 100 ° C. for 24 hours before being put into the extruder. The moisture content of the polycarbonate resin pellets after drying was 240 pm.
  • A-2 The polycarbonate resin pellets produced in Reference Example 2 were dried at 100 ° C for 24 hours before being put into the extruder. Polycarbonate after drying The water content of the resin pellet was 180 ppm.
  • A-3 The polycarbonate resin pellet produced in Reference Example 3 was dried for 24 hours at 100 before being put into the extruder. In addition, the water content of the poly strength monoponate resin pellets after drying was 180 ppm.
  • the resin composition of the present invention is excellent in heat resistance, thermal stability, moldability, hue and transparency.
  • the resin composition of the present invention contains a polycarbonate resin obtained by using at least one compound selected from the group consisting of a nitrogen-containing basic compound, an alkali metal compound, and an alkaline earth metal compound as a polymerization catalyst. Therefore, it excels in heat resistance and heat stability.
  • the resin composition of the present invention has a high biogenic substance content.
  • the molded product of the present invention is excellent in heat resistance, thermal stability, hue and transparency. Industrial applicability
  • the molded product of the present invention has good hue, transparency and mechanical properties, optical parts such as optical sheets, optical disks, information disks, optical lenses, prisms, various mechanical parts, building materials It can be widely used for various applications including automobile parts, various resin trays, and tableware.

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Abstract

L'invention porte sur une composition de résine de polycarbonate ayant une teneur élevée en matière biogène, qui présente d'excellentes propriétés de résistance à la chaleur, stabilité thermique, aptitude au moulage, teinte et transparence. De façon spécifique, l'invention porte sur une composition de résine contenant 0,0005-0,5 partie en poids d'au moins un stabilisant thermique (composant S) choisi dans le groupe constitué par les stabilisants au phosphore (PS) et les stabilisants phénols encombrés (HS) pour 100 parties en poids d'une résine de polycarbonate (composant A) contenant principalement une unité répétitive représentée par la formule (1) ci-après. De façon spécifique, l'invention porte également sur un article moulé d'une telle composition de résine.
PCT/JP2008/058298 2007-04-25 2008-04-23 Composition de résine de polycarbonate Ceased WO2008133342A1 (fr)

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CN2008800133557A CN101668813B (zh) 2007-04-25 2008-04-23 聚碳酸酯树脂组合物
US12/597,135 US8008381B2 (en) 2007-04-25 2008-04-23 Polycarbonate resin composition
JP2009511923A JP5323688B2 (ja) 2007-04-25 2008-04-23 ポリカーボネート樹脂組成物
EP08740966A EP2141202B1 (fr) 2007-04-25 2008-04-23 Composition de résine de polycarbonate

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US20110160406A1 (en) * 2009-12-30 2011-06-30 Sabic Innovative Plastics Ip B.V Blends of isosorbide-based copolycarbonate, method of making, and articles formed therefrom
JP2012131858A (ja) * 2010-12-20 2012-07-12 Toyota Central R&D Labs Inc ポリカーボネート樹脂組成物
JP2012214675A (ja) * 2010-06-25 2012-11-08 Mitsubishi Chemicals Corp ポリカーボネート樹脂組成物および成形品
EP2460856A4 (fr) * 2009-07-27 2013-01-02 Idemitsu Kosan Co Composition de résine de polycarbonate
KR20140009419A (ko) 2011-03-30 2014-01-22 미쓰비시 가가꾸 가부시키가이샤 폴리카보네이트 수지의 제조 방법
JP2015007248A (ja) * 2014-09-02 2015-01-15 帝人株式会社 ポリカーボネート樹脂ペレット
JP2015526581A (ja) * 2013-07-01 2015-09-10 エルジー・ケム・リミテッド ポリカーボネート樹脂組成物
JP2016027082A (ja) * 2014-06-27 2016-02-18 三菱化学株式会社 樹脂成形体の製造方法
JP2016028153A (ja) * 2008-11-28 2016-02-25 三菱化学株式会社 ポリカーボネート樹脂組成物、光学フィルム及びポリカーボネート樹脂成形品
JP2017048369A (ja) * 2015-09-04 2017-03-09 三菱エンジニアリングプラスチックス株式会社 芳香族ポリカーボネート樹脂組成物及びその成形品
WO2017038547A1 (fr) * 2015-09-04 2017-03-09 三菱エンジニアリングプラスチックス株式会社 Composition de résine de polycarbonate aromatique et produit moulé associé
KR101745036B1 (ko) * 2009-12-10 2017-06-08 데이진 가부시키가이샤 난연성 수지 조성물 및 그것으로부터의 성형품

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US8691915B2 (en) 2012-04-23 2014-04-08 Sabic Innovative Plastics Ip B.V. Copolymers and polymer blends having improved refractive indices
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EP2141202B1 (fr) 2013-02-27
JP5323688B2 (ja) 2013-10-23
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US8008381B2 (en) 2011-08-30
US20100076130A1 (en) 2010-03-25
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